1,384 Budgeting jobs in the United States

Description
My client, a $1B+ privately held design-build and systems integration company with both commercial and government contracts has a newly created position for a Corporate Budgeting Analyst due to their continued growth. This position will work closely with the Budget Manager and the Chief Accounting Officer and have a much more robust role than the title indicates. The Corporate Budgeting Analyst will be involved in corporate budgeting & planning and financial reporting as well as procurement, complex account reconciliations and various process automation and system implementation projects. The sky is limit in this diverse role with access and exposure to senior leadership and executives.
The position will include the following responsibilities, however not all will be introduced immediately or worked on daily, nor are all of these skills required to be selected for this position.
- Work with department leaders (VPs and Directors) to produce annual budget packages and supporting documentation for ~30 departments and consolidated
- Lead indirect procurement initiatives, including RFPs for company-wide blanket deals and manage rebate programs.
- Administer corporate budgeting and procurement controls.
- Perform month-end closing activities such as review of cost and analyze and report on budget fluctuations, prepaid and accrual reconciliations, and internal cost allocations.
- Work with internal programmers on automation of transactions, reporting, and reconciliations.
- Assist Chief Accounting Officer and CFO with Finance department and Corporate initiatives as they arise
- This requires coordination and communication not only within the Finance department, but more importantly with the Operating Divisions, other corporate departments, vendors and service providers.
- The company has a multi-layered operational financial reporting structure internal requirement, as well as approximately 50 subsidiaries including a growing international footprint adding complexities to the traditional financial reporting process, and approximately 30 departments
- Our objective is simplification and automation of repetitive entries and reconciliations.
- Perform more complex general ledger reconciliations, corporate allocations, and intercompany eliminations., including posting of adjusting journal entries as needed.
- Assist with preparation of monthly, quarterly, and annual financial statements.
- Assist with annual financial statement audit and corporate tax preparation.
- Job cost and percentage of completion and job cost accounting experience is helpful but can be learned.
This is an incredible opportunity for a candidate roughly 2-5 years into their career that has a strong foundation, outstanding ability to learn and apply new skills and desire to have a wide breadth of experience and grow within a company for the foreseeable future. My client has a tremendous culture and reputation of taking care of their employees on a variety of ways as evidenced by the long tenure of their employee population.
For consideration, please apply directly to this post. If you have additional questions, contact Lee Chernett, VP at Robert Half Finance & Accounting, via LinkedIn
Requirements
+ Bachelors degree in Finance, Accounting or related area of study
+ 2+ years of audit experience in a Top 20 CPA firm or GL accounting for a midsize/large company.
+ Desire to have a mix of both accounting and finance responsibilities
+ Outstanding interpersonal and communication skills
+ Track record of learning and applying new skills quickly and accurately
+ Project management experience (preferred)
+ Advanced Microsoft Excel skills (advanced formulas, budget models)
+ Strong foundation in accounting required (the finance side can be taught).
For consideration, please apply directly to this role. If you have additional questions, contact Lee Chernett, VP at Robert Half Finance & Accounting, via LinkedIn
Robert Half is the world's first and largest specialized talent solutions firm that connects highly qualified job seekers to opportunities at great companies. We offer contract, temporary and permanent placement solutions for finance and accounting, technology, marketing and creative, legal, and administrative and customer support roles.
Robert Half works to put you in the best position to succeed. We provide access to top jobs, competitive compensation and benefits, and free online training. Stay on top of every opportunity - whenever you choose - even on the go. Download the Robert Half app ( and get 1-tap apply, notifications of AI-matched jobs, and much more.
All applicants applying for U.S. job openings must be legally authorized to work in the United States. Benefits are available to contract/temporary professionals, including medical, vision, dental, and life and disability insurance. Hired contract/temporary professionals are also eligible to enroll in our company 401(k) plan. Visit roberthalf.gobenefits.net for more information.
© 2025 Robert Half. An Equal Opportunity Employer. M/F/Disability/Veterans. By clicking "Apply Now," you're agreeing to Robert Half's Terms of Use ( .

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Discover Impactful Work:**
Manage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.
Support the development of creative processes, methodologies, data, and technologies that will ensure ongoing improvements in the delivery SB&C services
**A day in the Life:**
+ Responsible for assigned country level SB&C function to develop, negotiate, administrate and execute assigned Clinical Trial Agreements and budgets.
+ Oversight of assigned country budget setup including parameters development.
+ Partner with Study Start up ManagersSB&C team, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and implement processes.
+ Ensure standards are applied to the SB&C processes across project portfolios and support continuous improvement activities while developing the process.
+ Partner with Study Startup, SB&C teamand Clinical Operations teams as an escalation point for global budget escalations outside of budget parameters.
+ Leverage leading industry tools and data sources to provide budget and contract feedback aligned with Takeda parameters and fair market value guidance.
+ Promptly recognize and improve potential delays providing solutions to resolve and escalate non-performance.
+ Manage site contracts and budgets negotiation timelines to ensure sites are "Ready To Enroll" to the Startup Project Plan.
**Keys to Success:**
**Education**
+ BS degree or international equivalent
**Experience,**
+ 4 or more years of experience in clincal research site contracting and budgeting, including country budget build with evidence of increasing responsibility within a pharmaceutical company, CRO or relevant industry vendor.
+ At least 2 years of site budgeting and contracting oversight
**Knowledge, Skills, Abilities**
+ Ability to explain data, facilitate decision making processes to be data driven.
+ Expertise in principles driving country/site budgeting and contracting strategies.
+ Excellent organizational skills, decision making, communication and negotiation skills.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
**Compensation and Benefits**
The salary pay range estimated for this position Trial Contracts Specialist III based inNorth Carolina is $75,800.00-$110,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
+ A choice of national medical and dental plans, and a national vision plan, including health incentive programs
+ Employee assistance and family support programs, including commuter benefits and tuition reimbursement
+ At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
+ Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
+ Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Discover Impactful Work:**
Manage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.
Support the development of creative processes, methodologies, data, and technologies that will ensure ongoing improvements in the delivery SB&C services
**A day in the Life:**
+ Responsible for assigned country level SB&C function to develop, negotiate, administrate and execute assigned Clinical Trial Agreements and budgets.
+ Oversight of assigned country budget setup including parameters development.
+ Partner with Study Start up ManagersSB&C team, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and implement processes.
+ Ensure standards are applied to the SB&C processes across project portfolios and support continuous improvement activities while developing the process.
+ Partner with Study Startup, SB&C teamand Clinical Operations teams as an escalation point for global budget escalations outside of budget parameters.
+ Leverage leading industry tools and data sources to provide budget and contract feedback aligned with Takeda parameters and fair market value guidance.
+ Promptly recognize and improve potential delays providing solutions to resolve and escalate non-performance.
+ Manage site contracts and budgets negotiation timelines to ensure sites are "Ready To Enroll" to the Startup Project Plan.
**Keys to Success:**
**Education**
+ BS degree or international equivalent
**Experience,**
+ 4 or more years of experience in clincal research site contracting and budgeting, including country budget build with evidence of increasing responsibility within a pharmaceutical company, CRO or relevant industry vendor.
+ At least 2 years of site budgeting and contracting oversight
**Knowledge, Skills, Abilities**
+ Ability to explain data, facilitate decision making processes to be data driven.
+ Expertise in principles driving country/site budgeting and contracting strategies.
+ Excellent organizational skills, decision making, communication and negotiation skills.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
**Compensation and Benefits**
The salary pay range estimated for this position Trial Contracts Specialist III based inNorth Carolina is $75,800.00-$110,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
+ A choice of national medical and dental plans, and a national vision plan, including health incentive programs
+ Employee assistance and family support programs, including commuter benefits and tuition reimbursement
+ At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
+ Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
+ Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Discover Impactful Work:**
Manage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.
Support the development of creative processes, methodologies, data, and technologies that will ensure ongoing improvements in the delivery SB&C services
**A day in the Life:**
+ Responsible for assigned country level SB&C function to develop, negotiate, administrate and execute assigned Clinical Trial Agreements and budgets.
+ Oversight of assigned country budget setup including parameters development.
+ Partner with Study Start up ManagersSB&C team, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and implement processes.
+ Ensure standards are applied to the SB&C processes across project portfolios and support continuous improvement activities while developing the process.
+ Partner with Study Startup, SB&C teamand Clinical Operations teams as an escalation point for global budget escalations outside of budget parameters.
+ Leverage leading industry tools and data sources to provide budget and contract feedback aligned with Takeda parameters and fair market value guidance.
+ Promptly recognize and improve potential delays providing solutions to resolve and escalate non-performance.
+ Manage site contracts and budgets negotiation timelines to ensure sites are "Ready To Enroll" to the Startup Project Plan.
**Keys to Success:**
**Education**
+ BS degree or international equivalent
**Experience,**
+ 4 or more years of experience in clincal research site contracting and budgeting, including country budget build with evidence of increasing responsibility within a pharmaceutical company, CRO or relevant industry vendor.
+ At least 2 years of site budgeting and contracting oversight
**Knowledge, Skills, Abilities**
+ Ability to explain data, facilitate decision making processes to be data driven.
+ Expertise in principles driving country/site budgeting and contracting strategies.
+ Excellent organizational skills, decision making, communication and negotiation skills.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
**Compensation and Benefits**
The salary pay range estimated for this position Trial Contracts Specialist III based inNorth Carolina is $75,800.00-$110,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
+ A choice of national medical and dental plans, and a national vision plan, including health incentive programs
+ Employee assistance and family support programs, including commuter benefits and tuition reimbursement
+ At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
+ Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
+ Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Discover Impactful Work:**
Manage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.
Support the development of creative processes, methodologies, data, and technologies that will ensure ongoing improvements in the delivery SB&C services
**A day in the Life:**
+ Responsible for assigned country level SB&C function to develop, negotiate, administrate and execute assigned Clinical Trial Agreements and budgets.
+ Oversight of assigned country budget setup including parameters development.
+ Partner with Study Start up ManagersSB&C team, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and implement processes.
+ Ensure standards are applied to the SB&C processes across project portfolios and support continuous improvement activities while developing the process.
+ Partner with Study Startup, SB&C teamand Clinical Operations teams as an escalation point for global budget escalations outside of budget parameters.
+ Leverage leading industry tools and data sources to provide budget and contract feedback aligned with Takeda parameters and fair market value guidance.
+ Promptly recognize and improve potential delays providing solutions to resolve and escalate non-performance.
+ Manage site contracts and budgets negotiation timelines to ensure sites are "Ready To Enroll" to the Startup Project Plan.
**Keys to Success:**
**Education**
+ BS degree or international equivalent
**Experience,**
+ 4 or more years of experience in clincal research site contracting and budgeting, including country budget build with evidence of increasing responsibility within a pharmaceutical company, CRO or relevant industry vendor.
+ At least 2 years of site budgeting and contracting oversight
**Knowledge, Skills, Abilities**
+ Ability to explain data, facilitate decision making processes to be data driven.
+ Expertise in principles driving country/site budgeting and contracting strategies.
+ Excellent organizational skills, decision making, communication and negotiation skills.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
**Compensation and Benefits**
The salary pay range estimated for this position Trial Contracts Specialist III based inNorth Carolina is $75,800.00-$110,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
+ A choice of national medical and dental plans, and a national vision plan, including health incentive programs
+ Employee assistance and family support programs, including commuter benefits and tuition reimbursement
+ At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
+ Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
+ Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
**At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.**
**Discover Impactful Work:**
**Handle escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.**
**Support the development of creative processes, methodologies, data, and technologies that will ensure ongoing improvements in the delivery SB&C services**
**A day in the Life:**
**Responsible for assigned country level SB&C function to develop, negotiate, administrate and execute assigned Clinical Trial Agreements and budgets.**
**Oversight of assigned country budget setup including parameters development.**
**Partner with Study Start up Managers SB&C team, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and implement processes.**
**Ensure standards are applied to the SB&C processes across project portfolios and support continuous improvement activities while developing the process.**
**Partner with Study Startup, SB&C teaming Clinical Operations teams as an escalation point for global budget escalations outside of budget parameters.**
**Leverage leading industry tools and data sources to provide budget and contract feedback aligned with Takeda parameters and fair market value mentorship.**
**Promptly recognize and improve potential delays providing solutions to resolve and escalate non-performance.**
**Lead site contracts and budgets negotiation timelines to ensure sites are "Ready To Enroll" to the Startup Project Plan.**
**Keys to Success:**
**Education**
**BS degree or international equivalent**
**Experience,**
**4 or more years of experience in clincal research site contracting and budgeting, including country budget build with evidence of growing responsibility within a pharmaceutical company, CRO or relevant industry vendor.**
**At least 2 years of site budgeting and contracting oversight**
**Knowledge, Skills, Abilities**
**Ability to explain data, facilitate decision making processes to be data driven.**
**Expertise in principles driving country/site budgeting and contracting strategies.**
**Excellent social skills, decision making, communication and negotiation skills.**
**In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.**
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Discover Impactful Work:**
Manage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.
Support the development of creative processes, methodologies, data, and technologies that will ensure ongoing improvements in the delivery SB&C services
**A day in the Life:**
+ Responsible for assigned country level SB&C function to develop, negotiate, administrate and execute assigned Clinical Trial Agreements and budgets.
+ Oversight of assigned country budget setup including parameters development.
+ Partner with Study Start up ManagersSB&C team, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and implement processes.
+ Ensure standards are applied to the SB&C processes across project portfolios and support continuous improvement activities while developing the process.
+ Partner with Study Startup, SB&C teamand Clinical Operations teams as an escalation point for global budget escalations outside of budget parameters.
+ Leverage leading industry tools and data sources to provide budget and contract feedback aligned with Takeda parameters and fair market value guidance.
+ Promptly recognize and improve potential delays providing solutions to resolve and escalate non-performance.
+ Manage site contracts and budgets negotiation timelines to ensure sites are "Ready To Enroll" to the Startup Project Plan.
**Keys to Success:**
**Education**
+ BS degree or international equivalent
**Experience,**
+ 4 or more years of experience in clincal research site contracting and budgeting, including country budget build with evidence of increasing responsibility within a pharmaceutical company, CRO or relevant industry vendor.
+ At least 2 years of site budgeting and contracting oversight
**Knowledge, Skills, Abilities**
+ Ability to explain data, facilitate decision making processes to be data driven.
+ Expertise in principles driving country/site budgeting and contracting strategies.
+ Excellent organizational skills, decision making, communication and negotiation skills.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
**Compensation and Benefits**
The salary pay range estimated for this position Trial Contracts Specialist III based inNorth Carolina is $75,800.00-$110,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
+ A choice of national medical and dental plans, and a national vision plan, including health incentive programs
+ Employee assistance and family support programs, including commuter benefits and tuition reimbursement
+ At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
+ Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
+ Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Discover Impactful Work:**
Manage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.
Support the development of creative processes, methodologies, data, and technologies that will ensure ongoing improvements in the delivery SB&C services
**A day in the Life:**
+ Responsible for assigned country level SB&C function to develop, negotiate, administrate and execute assigned Clinical Trial Agreements and budgets.
+ Oversight of assigned country budget setup including parameters development.
+ Partner with Study Start up ManagersSB&C team, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and implement processes.
+ Ensure standards are applied to the SB&C processes across project portfolios and support continuous improvement activities while developing the process.
+ Partner with Study Startup, SB&C teamand Clinical Operations teams as an escalation point for global budget escalations outside of budget parameters.
+ Leverage leading industry tools and data sources to provide budget and contract feedback aligned with Takeda parameters and fair market value guidance.
+ Promptly recognize and improve potential delays providing solutions to resolve and escalate non-performance.
+ Manage site contracts and budgets negotiation timelines to ensure sites are "Ready To Enroll" to the Startup Project Plan.
**Keys to Success:**
**Education**
+ BS degree or international equivalent
**Experience,**
+ 4 or more years of experience in clincal research site contracting and budgeting, including country budget build with evidence of increasing responsibility within a pharmaceutical company, CRO or relevant industry vendor.
+ At least 2 years of site budgeting and contracting oversight
**Knowledge, Skills, Abilities**
+ Ability to explain data, facilitate decision making processes to be data driven.
+ Expertise in principles driving country/site budgeting and contracting strategies.
+ Excellent organizational skills, decision making, communication and negotiation skills.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
**Compensation and Benefits**
The salary pay range estimated for this position Trial Contracts Specialist III based inNorth Carolina is $75,800.00-$110,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
+ A choice of national medical and dental plans, and a national vision plan, including health incentive programs
+ Employee assistance and family support programs, including commuter benefits and tuition reimbursement
+ At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
+ Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
+ Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Discover Impactful Work:**
Manage escalations and review of assigned site budgets and contracts to ensure timely contract execution and study startup forecasts are achieved.
Support the development of creative processes, methodologies, data, and technologies that will ensure ongoing improvements in the delivery SB&C services
**A day in the Life:**
+ Responsible for assigned country level SB&C function to develop, negotiate, administrate and execute assigned Clinical Trial Agreements and budgets.
+ Oversight of assigned country budget setup including parameters development.
+ Partner with Study Start up ManagersSB&C team, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and implement processes.
+ Ensure standards are applied to the SB&C processes across project portfolios and support continuous improvement activities while developing the process.
+ Partner with Study Startup, SB&C teamand Clinical Operations teams as an escalation point for global budget escalations outside of budget parameters.
+ Leverage leading industry tools and data sources to provide budget and contract feedback aligned with Takeda parameters and fair market value guidance.
+ Promptly recognize and improve potential delays providing solutions to resolve and escalate non-performance.
+ Manage site contracts and budgets negotiation timelines to ensure sites are "Ready To Enroll" to the Startup Project Plan.
**Keys to Success:**
**Education**
+ BS degree or international equivalent
**Experience,**
+ 4 or more years of experience in clincal research site contracting and budgeting, including country budget build with evidence of increasing responsibility within a pharmaceutical company, CRO or relevant industry vendor.
+ At least 2 years of site budgeting and contracting oversight
**Knowledge, Skills, Abilities**
+ Ability to explain data, facilitate decision making processes to be data driven.
+ Expertise in principles driving country/site budgeting and contracting strategies.
+ Excellent organizational skills, decision making, communication and negotiation skills.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
**Compensation and Benefits**
The salary pay range estimated for this position Trial Contracts Specialist III based inNorth Carolina is $75,800.00-$110,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
+ A choice of national medical and dental plans, and a national vision plan, including health incentive programs
+ Employee assistance and family support programs, including commuter benefits and tuition reimbursement
+ At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
+ Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
+ Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.